N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propane-2-sulfonamide
95%
- Product Code: 83588
CAS:
2155834-10-7
| Molecular Weight: | 325.23136 g./mol | Molecular Formula: | C₁₅H₂₄BNO₄S |
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| EC Number: | MDL Number: | MFCD31916412 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it finds application in the development of boron-containing compounds for potential use in medicinal chemistry, such as enzyme inhibitors or receptor modulators. Its sulfonamide moiety further enhances its utility in drug design by contributing to interactions with biological targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $701.64 |
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| 1.000 | 10-20 days | $2,028.84 |
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N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propane-2-sulfonamide
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it finds application in the development of boron-containing compounds for potential use in medicinal chemistry, such as enzyme inhibitors or receptor modulators. Its sulfonamide moiety further enhances its utility in drug design by contributing to interactions with biological targets.
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